JustJoe
New Member
I used all my GSH raws. I was aiming for 600mg then diluted it too much using too weak NaOH during ph bal.What displacement are u using? ~.7?
Why not just do a 700mg/ml and pin less liquid.
At 800mg/ml i could not push through a .22 filter
Can that EDTA be filtered out?
Isn't that a chelation agent?
I kind of want the EDTA to completely dissolve.
I’m (attempting) using L-Histadine as a buffer instead of PBS, PBS=pip for me; EDTA as a chelator (binds to any trace heavy metals and makes them water soluble and tissue inactive, washing out through kidneys), and Sodium Metabisufite (SMB) and BA 0.9 as a preservatives.
l-Histadine is a completely pain free buffer, used on some vaccines.
When I get more raws, make it work, and check the PIP, I’ll post the formulation.
Here’s a cool quick read:
This one talks more about L Histadine as buffer:
Histidine in Health and Disease: Metabolism, Physiological Importance, and Use as a Supplement - PMC
L-histidine (HIS) is an essential amino acid with unique roles in proton buffering, metal ion chelation, scavenging of reactive oxygen and nitrogen species, erythropoiesis, and the histaminergic system. Several HIS-rich proteins (e.g., ...


